Data Entry Coordinator

Title: Data Entry Coordinator Location: Miami, FL About us: Clinical Pharmacology of Miami (CPMI) is a dynamic and growing Phase I Clinical Trials Site committed to fostering a positive work environment and driving business success through our people. We are looking for a Data Entry Coordinator to join our team and help us continue to build a high-performance culture that aligns with our business objectives. Job Description: The Data Entry Coordinator is responsible for the overall coordination, organization, and efficient implementation of clinical data. Complete all study related data entry procedures under the direction of the Site Director. Maintain accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Clinical Data Entry Coordinator is guided by Good Clinical Practices (GCP), International Conference on Harmonization (ICH) guidelines, and company standard operating procedures and policies. Responsibilities: Responsible for clinical data processing as directed by Site Director or another assignedmanager. Quality control the clinical data to ensure the data quality and report discrepancies to thecoordinator. Complete any training as required by sponsor for access and approval to complete data entry. Enter data as appropriate for protocol into paper or electronic case reportforms. Track to ensure that data entry is complete for subjects including completed study visits and related forms. With CRC and/or manager oversight assist Sponsor or CRO data manager with resolution of queries to ensure clinical data quality. Study, learn, and comply with ERG standard operating procedures and other policies, practices, and regulations where applicable. Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERGs objectives. Skills and Qualifications: Education and experience High School Diploma or equivalent Understandregulatory requirements, as well as Good Clinical Practices (GCP) and International Conference on Harmonization (ICH) guidelines. Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner. Knowledgeable in medical terminology to communicate with physician office and staff. Able to initiate or modify behavior to achieve desired outcomes despite environmental factors, priorities, or problems that might not be well defined or that are subject to change. Requirements Excellent communication skills (interpersonal, written, verbal) Must be able to identify and communicate about research problems and processes across various levels of theorganization. Good organizational and interpersonal skills Attention todetail. Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)